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LOCAS: multilabel mRNA localization with supervised contrastive learning.

Abrar Rahman Abir1, Md Toki Tahmid1, M Saifur Rahman1

  • 1Department of Computer Science and Engineering, Bangladesh University of Engineering and Technology, Dhaka-1000, Bangladesh.

Briefings in Bioinformatics
|August 27, 2025
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Summary
This summary is machine-generated.

This study introduces LOCAS, a new deep learning method for predicting messenger RNA (mRNA) subcellular localization. LOCAS improves accuracy by learning RNA sequence representations and relationships between multiple localization sites.

Keywords:
RNA language modelcontrastive learningmRNA subcellular localization

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Area of Science:

  • Computational biology
  • Molecular biology
  • Bioinformatics

Background:

  • Messenger RNA (mRNA) subcellular localization is vital for gene regulation and protein synthesis control.
  • Existing computational methods often use single-label classification, failing to address the multi-label nature of mRNA localization.
  • Current deep learning approaches struggle to model relationships between multiple mRNA localization sites.

Purpose of the Study:

  • To develop a novel computational framework, Localization with Supervised Contrastive Learning (LOCAS), for accurate multi-label mRNA subcellular localization prediction.
  • To enhance the modeling of relationships between multiple localization sites using supervised contrastive learning.
  • To improve the precision of spatial and temporal control of protein synthesis through better mRNA localization prediction.

Main Methods:

  • Integration of an RNA language model (RiNALMo) for high-quality sequence embeddings.
  • Application of supervised contrastive learning (SCL) to refine embedding spaces and ensure biologically meaningful clustering.
  • Introduction of an overlap-threshold-based similarity measure to handle overlapping localization labels.
  • Utilization of an ML-Decoder with a cross-attention mechanism for enhanced multi-label classification.

Main Results:

  • LOCAS achieved state-of-the-art performance on the RNALocate and RNALocate V2.0 benchmark datasets across all evaluation metrics.
  • Ablation studies confirmed the significant contributions of contrastive learning and the ML-decoder to improved multi-label classification accuracy.
  • The proposed method effectively models relationships between multiple mRNA localization sites.

Conclusions:

  • LOCAS provides a powerful and scalable solution for multi-label mRNA subcellular localization prediction.
  • Integrating RNA sequence representation learning with SCL significantly advances the field of mRNA localization prediction.
  • The findings pave the way for more precise understanding and control of gene expression through accurate mRNA localization.